Novel process for solubilizing protein from a proteinaceous material and compositions thereof

ABSTRACT

The process for solubilizing proteinaceous material of the present invention includes subjecting the proteinaceous material to a sufficient amount of a basic solution to obtain a supernatant that has a basic pH and exposing the supernatant to the basic solution for a sufficient length of time and temperature for hydrolysis to occur. The process also includes cooling the mixture of the supernatant and proteinaceous material and optionally acidifying the mixture. This process may also include recovering the solubilized protein from the supernatant for use in various applications. Also provided herein is a composition of solubilized proteins from eggshell membrane obtained using processes of the present invention.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Divisional Application of 12/253,719 filed Oct.17, 2008, which claims priority under 35 U.S.C. §119 of a provisionalapplication Ser. No. 60/980,607 filed Oct. 17, 1997, which applicationsare hereby incorporated by reference in their entirety.

BACKGROUND OF THE INVENTION

Many industrial waste products such as pigskin, fish scale, and avianeggshell membranes are a source of valuable bioactive materials,including collagen, that have widespread applications in medical, healthand cosmetic industries. To date, a major drawback to their use has beenthe difficulty in solubilizing these proteinaceous starting materials ina sufficiently stable and active pure form at an industrial scale sothat high yield is achieved in an economic manner.

For example, solubilization of eggshell membranes has proven technicallydifficult. Recent processes to solubilize eggshell membranes include theuse of mercaptopropionic acid, various extraction agents, or enzymes,such as peptidases, trypsin, and collagenases; however, problems havebeen associated with these procedures. The amount of protein solubilizedfrom the starting material by these processes is low, the techniques arenot cost-effective, and often the recovered protein components do notmaintain their native activity. Therefore an inexpensive process forsolubilizing eggshell membranes and other sources of proteinaceousmaterials while maintaining both yield, purity and activity of thesolubilized protein is needed, particularly one suited for commercialscale implementation.

BRIEF SUMMARY OF THE INVENTION

The present invention relates to a process to provide forcommercial-scale solubilization of various components from aproteinaceous material such as eggshell membranes. As a result of thepresent invention, one can produce a composition having large amounts ofsolubilized proteins from eggshell membranes. This process has anadditional advantage in that the resulting composition may be used as asource for the isolation of other valuable components. Specificcomponents, such as individual proteins, may be further purified fromthe composition thereby making it feasible to isolate proteins ofinterest from the composition.

The process for solubilizing proteinaceous material of the presentinvention includes subjecting the proteinaceous material to a sufficientamount of a basic solution for a sufficient length of time andtemperature for hydrolysis to occur. The process also includes coolingthe mixture of proteinaceous material/basic solution, and, if desiredacidifying the mixture, to obtain solubilized proteins. This process mayalso include recovering the solubilized proteins from the mixture foruse in various applications.

Therefore it is a primary object feature or advantage of the presentinvention to improve over the state of the art.

A further object, feature, or advantage of the invention is to provide anovel process for the solubilization of a proteinaceous material.

A further object, feature, or advantage of the invention is to provide aprocess for the solubilization of a proteinaceous material that producessolubilized protein that can be used in medical, cosmetic, pharmaceutic,dermatological or nutritional applications.

Another object, feature, or advantage of the invention is to provide aprocess for the solubilization of a proteinaceous material thatsubstantially lowers the mineral (ash) content of the solubilizedprotein composition.

Yet another object, feature, or advantage of the invention is to providea process for the solubilization of a proteinaceous material thatincreases the yield of the solubilized protein composition.

An object, feature, or advantage of the present invention is to providea means to solubilize proteins from eggshell membranes.

It is a further object, feature, or advantage of the present inventionis to provide a composition of solubilized proteins from eggshellmembranes.

Yet another object, feature, or advantage of the invention is to providea composition that is rich in proteins solubilized from eggshellmembranes. Still another object, feature, or advantage of the inventionis to provide a cosmetic, medical, pharmaceutic, dermatological, ornutritional composition that is rich in proteins solubilized fromeggshell membranes.

An object, feature, or advantage of the present invention is to providea composition useful in treating an individual in need of proteinssolubilized from eggshell membranes.

An additional object, feature, or advantage of the present invention isto provide a method of treating an individual in need of proteinssolubilized from eggshell membranes.

A further object, feature, or advantage of the present invention is toprovide a process for preparing a composition that has solubilizedproteins obtained from an eggshell membrane.

A still further object, feature, or advantage of the present inventionis to provide a process which is suitable for implementation on acommercial/industrial scale.

One or more of these and/or other objects, features, or advantages ofthe present invention will become apparent from the specification andclaims that follow. No single embodiment of the invention need fulfillall or any of the objects stated herein.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a flow chart for one embodiment of a process for solubilizingeggshell membranes.

FIG. 2 is a flow chart for one embodiment of a process for solubilizingeggshell membranes.

FIGS. 3A and 3B are flow charts for one embodiment of a process forsolubilizing eggshell membranes.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention belongs. Unless mentioned otherwise, thetechniques employed or contemplated herein are standard methodologieswell known to one of ordinary skill in the art. The materials, processesand examples are illustrative only and not limiting. The following ispresented by way of illustration and is not intended to limit the scopeof the invention.

Many modifications and other embodiments of the inventions set forthherein will come to mind to one skilled in the art to which theseinventions pertain having the benefit of the teachings presented in theforegoing descriptions and the associated drawings. Therefore, it is tobe understood that the inventions are not to be limited to the specificembodiments disclosed and that modifications and other embodiments areintended to be included within the scope of the appended claims.

To date, a composition containing proteins solubilized from eggshellmembrane has not been obtainable on a commercial scale due to lengthyprocedures, low yield of proteins and polysaccharides, or lack ofbioactivity of isolated proteins. There is no known process for thepreparation of a composition from eggshell membrane that overcomescurrent technical difficulties and produces a high yield, solubilizedprotein composition which is highly pure and undenaturated. Thesolubilized composition obtained by the process of the present inventionhas surprising levels of proteins, polysaccharides, and amino acids, isessentially free of odor, and can be efficiently prepared.Advantageously, since proteolytic enzymes or cross-linking agents arenot used, processes of the present invention are also more economic thanthose of current practices.

The process of the invention is suited for solubilization of proteinfrom various proteinaceous materials. Any suitable proteinaceousmaterial may be employed in the practice of the present invention. Asused herein, the term “proteinaceous material” is used to describe amaterial comprising proteins, polypeptides or peptides. Proteinaceousmaterials may be obtained and prepared from any number of resources.Examples include but are not limited to connective tissues, such as thecombs of roosters, avian eggshell membranes, skin, fishscale, flesh, orcartilage. As used herein, the term “eggshell membrane” refers to anypart of the eggshell membrane, for example, the inner eggshell membrane,the outer eggshell membrane or both. The eggshell membrane also includesthe eggshell membrane in its various forms, for example, frozen, raw(wet) or dried.

Avian eggshell membranes are conventionally considered a waste productdue in part to both the difficulties encountered in separating theeggshell membrane from the eggshell and further in the difficulties inprocessing the eggshell membrane in a manner that will result inobtaining proteins, polypeptides or peptides of interest. Variousmeasures of the protein content of eggshell membranes are present in theprior art.

Examples of one measure of the amount of protein and individual aminoacids known to be found in egg shell membranes are shown below from U.S.Pat. No. 6,899,294 to MacNeil.

Protein And Individual Amino Acids in Eggshell Membranes % Protein 85Lysine 3.35 Histidine 3.48 Arginine 6.46 Threonine 4.60 Glutamic Acid9.70 Proline 9.34 Glysine 4.94 Cysteine 8.50 Valine 6.30 Methionine 3.09Isoleucine 3.19 Leucine 4.30 Tyrosine 1.73 Phenylalanine 1.65

Another measure of the typical amino acid composition of egg shellmembranes is provided by U.S. patent application Ser. No. 10/797,747,published patent application no. 20040180025 (Long et al.) and is setforth in the below table:

Typical Amino Acid Composition of Eggshell Membrane Protein % Lysine2.88 Tryptophan 2.51 Leucine 3.85 Aspartic Acid 7.01 Proline 8.23Isoleucine 2.01 Threonine 4.42 Glycine 3.99 Histidine 2.79 Arginine 5.33Tyrosine 1.33 Glutamic Acid 8.23 Cystine 6.01 Alanine 2.00 Methionine2.85 Valine 5.13 Phenylalanine 1.48 Serine 4.28

Another measure of the constituents of egg shell membranes (inpercentage) is provided by Long et al and is set forth in the belowtable:

Typical Constituents of Eggshell Membrane % Collagen 35 Glucosamine 10Chondroitin  9 Hyaluronic acid 5-10

Prior testing on avian egg shell membranes with a particular process isdescribed in U.S. patent application Ser. No. 11/471,766, publishedpatent application no. 20070017447 entitled Avian Eggshell MembranePolypeptide Extraction Via Fermentation Process. That testing resultedin the following composition:

Constituent % Protein 90.08 Aspartic Acid 7.98 Threonine 5.19 Serine5.05 Glutamic Acid 11.91 Proline 10.79 Glycine 5.43 Alanine 2.46 Valine6.02 Isoleucine 2.91 Leucine 4.19 Tyrosine 1.57 Phenylalanine 1.60Lysine 3.21 Histidine 3.38 Arginine 6.89 Cystine 6.72 Methionine 3.50Tryptophan 3.64

Thus, there are numerous types of proteins, polypeptides, and peptidesin eggshell membranes that can be extracted provided that the membranescan be solubilized. The eggshell membrane may be obtained from anynumber of resources, including an egg-breaking facility. The eggshellmembrane may be separated from the egg white and eggshell using anysuitable technique, for example mechanical or chemical methods or acombination of methods. For example, unseparated eggshells may beprocessed as described in U.S. patent application Ser. No. 11/333,697,published application no. 20060159816, herein incorporated by referencein its entirety. The eggshell membrane separation method includesplacing the unseparated eggshells in a fluid tank containing a fluidmixture, such as a mixture of distilled water and acetic acid, andapplying cavitation to thereby assist in separating the eggshellmembranes from the eggshells. The eggshell membranes may then berecovered using any suitable technique, preferably the separationprocess does not damage or denature the proteins. The isolated eggshellmembrane may be processed as described herein. For example, the eggshellmembranes may be subjected to a solubilization process for solubilizingat least one type of polypeptide or polysaccharide from the eggshellmembranes. Components of interest that may be solubilized include butare not limited to collagen, elastin, desmosine, lysozyme, glucosamine,chondroitin, ovotransferrin, B-N-acetylglucosaminidase, hyaluronic acid,amino acids or other components of interest. The collagen may be Type Icollagen, Type V collagen, Type X collagen or combinations thereof. Thecomponents may be solubilized from the eggshell membrane and purifiedfor numerous uses.

As shown in FIG. 1, in one embodiment, the process of the presentinvention includes subjecting a proteinaceous material such as eggshellmembrane to a sufficient amount of a basic solution so that hydrolysisof the eggshell membrane occurs. The basic solution is added to theeggshell membrane to produce a supernatant having a basic pH. As usedherein, the term basic refers to a pH greater than 7. The pH of thesupernatant may be adjusted to a pH of from about 9.0 to a pH of fromabout 11.5, preferably from a pH range of from about 10.5 to about 11.5.Any suitable basic solution may be used including but not limited tosodium hydroxide, potassium hydroxide, and calcium hydroxide. Thesufficient amount of basic solution to add to the proteinaceous materialmay be determined in any number of ways as appreciated by those skilledin the art. For example, the sufficient amount of the basic solutionnecessary to achieve a pH from about 9.0 to about 11.5 may be determinedbased on the total weight of the proteinaceous material, preferablybased on the solid (dry) weight of the proteinaceous material, and themolarity of the basic solution. It is preferred that the temperature andpH be closely monitored, so that functional proteins, polypeptides andpeptides are obtained rather than mostly amino acids. As used herein, a“polypeptide”, “peptide” or “protein” are used interchangeably. In oneaspect, the process includes exposing the supernatant to the basicsolution for a sufficient length of time and temperature for hydrolysisto occur. One skilled in the art will appreciate that the time neededfor the hydrolysis reaction of the proteinaceous material to proceedwill vary in part based on the temperature selected. Accordingly,hydrolysis of the proteinaceous material may be carried out at anysuitable temperature for any suitable length of time, for example, thetemperature may be from a range of about 30° C. to about 65° C.,preferably from a temperature of about 45° C. to about 60° C., and morepreferably from a temperature of at least about 50° C. The hydrolysistime can be as long as necessary to achieve the desired result. Thelength of time the proteinaceous material is subjected to hydrolysis mayvary from as little as hours, such as 3 to 24 hours, to days dependingon the temperature and other conditions used. For example, use of ahigher temperature, for example of 50° C. compared to 30° C., andstirring the mixture of proteinaceous material/basic solution wouldreduce the length of time needed for hydrolysis reaction to occur. Oneskilled in the art can monitor the progress of the hydrolysis reactionusing standard techniques such as trichloroacetic acid (TCA) proteinprecipitation and/or visualization methods. For example, one could takea sample of the supernatant, precipitate proteins out using TCA, andanalyze the supernatant after TCA precipitation for levels of nitrogen(indicative of free amino acids). Alternately, hydrolysis may bemonitored by using simple visualization methods over selected timeintervals. Typically, measurements are performed about three hours aftersubjecting the proteinaceous material to the basic solution to assesshydrolysis of the proteinaceous material into soluble proteins. A samplemay be taken from the proteinaceous material/basic solution mixture andthe sample analyzed for the presence of insoluble proteins of theeggshell membrane. Samples are spun down using centrifugation and thecontents visually analyzed for the presence of a yellow material ofnon-hydrolyzed eggshell membranes, i.e. insoluble eggshell membraneproteins. It is noted that spun down samples may also contain eggshellparticulates which are white in color. If the yellow material ofinsoluble eggshell membrane proteins is observed then the hydrolysisreaction is allowed to proceed and samples from the mixture are taken at15 to 20 minute intervals thereafter and evaluated. Typically, thereaction is allowed to proceed until the yellow insoluble proteins areno longer present in the spun down samples. Thus, one skilled in the artcan determine whether the proteinaceous material has been substantiallyhydrolyzed, whether more time is needed or whether the reaction hasproceeded too long as indicated by the hydrolysis of the proteins intoamino acids.

In one aspect, the process of the invention includes cooling thesupernatant. For example, the temperature of the supernatant comprisingthe hydrolyzed proteinaceous material may be adjusted to a temperatureof from about 2° C. to about 18° C., more preferably to a temperature ofabout 2° C. to about 7° C.

In another aspect, the process includes the removal of particulates,such as eggshells or fine calcium from eggshells, from the supernatantcontaining the hydrolyzed proteinaceous material by any suitableseparation technique. This may be accomplished in any number of ways,including, but not limited to centrifugation, ultra-centrifugation,filtration or microfiltration, or combinations of separation techniques.For example, centrifugation may be used to separate particulates fromthe supernatant containing the hydrolyzed proteinaceous material and thesupernatant removed by decanting, pumping, and the like. Any number offiltration techniques may be used for the process of the presentinvention, including but not limited to gravity filtration, pressurefiltration, vacuum filtration, batch filtration, membrane filtration,filter press, continuous filtration, or any suitable combination.Filtration may include the use of any suitable filter that is capable ofremoving particulates from the supernatant. A suitable filter mayinclude but is not limited to a drum filter, a disk filter, filter pressor a sock filter. Preferably, a filter sock with a 100 micron to 865micron sock size is used. The filter may be made from a variety ofmaterials such as, but not limited to, sintered-metal, cloth, polymericfiber, natural fiber, paper such as a coffee filter, metal mesh, pulp,ceramic, or a combination of the foregoing materials, and the like. Thepore size of the filter may be of any size so long as it filters out thedesired particulates. The range of pore size may be from of 0.01micrometers to 100-200 micrometers, or greater.

The resulting solubilized components in the supernatant can be furtherpurified, isolated, and/or concentrated. For example, in one aspect, theprocess of the present invention includes removing salt (ash) orminerals from the supernatant. The relative amount of salts/minerals inthe supernatant can be determined using any suitable technique includingmeasuring the conductivity of the supernatant, using, for example, ameter to measure conductivity in milliSiemens(mS), ppm, ampre/volts,etc. The level of salt in the supernatant can be adjusted so that thefinal solubilized composition has the desired or acceptable level orpercentage of ash, depending on the intended use for the resultingsolubilized composition and the industry standards.

For example, with respect to the solubilization of avian eggshellmembranes, a conductivity of a supernatant that is at or above 5milliSiemens/cm may be considered to be a high level of salt/mineral. Ifthe salt/mineral content in the supernatant is not reduced, it willbecome ash in the resulting solubilized composition. Ash is undesirablebecause it is potentially perceived as a “filler” in the consumedproduct. Additionally, many health conscious consumers may desire tolimit their consumption of salt. The reduction in the amount of ash inthe supernatant increases the percentage of protein content in therecovered solubilized composition.

If the supernatant has a conductivity that would result in thesolubilized protein composition having an ash content that isunacceptable, salts/minerals may be removed from the supernatant untilan acceptable level of salt is present in the supernatant. In somecases, a supernatant having less than 5 milliSiemens/cm (mS/cm) isacceptable, preferably 4 or less mS/cm, more preferably from about 2 toabout 4 mS/cm. The salt/minerals may be removed from the supernatantusing any suitable process, for example, filtration, dialysis or ionexchange. The process may include separating the hydrolyzed proteins inthe supernatant from salt and if desired, specific molecules, using amembrane. The separation may be performed using any suitable technique,such as the use of a membrane. This also allows for the concentration ofa composition that has high levels of solubilized proteins. Thecomposition may also contain polysaccharides. Any process that allowsfor concentration may be used, although, preferably the concentrationprocess maintains the biological activities of the composition or of theindividual components in the composition. Typically, the supernatantsare passed through a membrane having the desired nominal molecularweight cut-off value, leaving solubilized proteins and other solubilizedcomponents having a molecular weight larger than the cut-off valuebehind. In one embodiment, a membrane with a nominal molecular weightcut-off value of about 1000-3000 Daltons is used, resulting in acomposition that has high amounts of solubilized proteins, but allowingamino acids and other small molecules to pass through. If desired, theamino acids may be recovered from the supernatant for use in any numberof applications, such as consumable products. If desired, a specificcomponent or a mixture of specific components in the solubilizedcomposition may be isolated. Solubilized components may be isolated inany manner that is convenient. As appreciated by those ordinarilyskilled in the art, the selection of membrane size can be used to obtaina composition enriched for a particular size of protein or population ofproteins. For example, use of a membrane having a nominal molecularweight cut-off value of about 100 kDa may be used to isolate elastin andother solubilized proteins larger than 100 kDa and proteins that areless than 100 kDa such as collagen and desmosine. Desmosine, ananti-oxidant of three amino acid residues of lysine, may be releasedwhen the elastin is solubilized, and if desired, may be furtherconcentrated using a membrane having a nominal molecular weight cut-offvalue of less than 500 molecular wt.

Advantageously, filtering and/or performing dialysis of the supernatantmay remove sulfur compounds from the supernatant, thereby reducing thesulfur odor of the supernatant. In another aspect, the process of theinvention may include removing odor causing components from thesupernatant, for example, by using a filter with an odor-absorbingcompound such as a charcoal filter or an activated carbon filter.Additionally, an odor-reacting compound that is an oxidizing agent, suchas hydrogen peroxide, may be added to the supernatant to reduce sulfurodors. The process may also include reducing the number ofmicroorganisms in the supernatant by subjecting the supernatant tofiltration, for example, a 0.8 micrometer filter.

In another aspect, the process includes adjusting the pH of thesupernatant or permeate comprising the hydrolyzed proteins so that thesupernatant or permeate has a pH from about 6.0 to about 8.0, preferablyto a pH of about 7.0. The pH may be adjusted using any suitable acidicsolution that has a pH of less than 7, including but not limited to asolution of acetic, oxalic, phosphoric, chloroacetic, citric, formic,benzoic, oxalic, succinic, acetic, propionic hydrochloric, nitric,sulfuric, hydrotropic, hydrologic, perchloric, chloric, phosphoric, orsulfurous acid or combinations thereof. In one embodiment, the pH andthe temperature of the supernatant or permeate are loweredsimultaneously or consecutively, although it is preferred that thesupernatant be cooled prior to addition of the acidic solution.

In a preferred embodiment, the removal of salts, for example, bydialysis, pH adjustment of the supernatant or permeate from a basic pHto a pH of about 7.0, and removal of sulfur odor using hydrogen peroxideare performed simultaneously. As appreciated by one skilled in the art,these steps may be performed consecutively, in a different order, oromitted and still yield a composition of solubilized proteins.

The solubilized composition resulting from the process of the presentinvention may be prepared in any number of forms or formulations. In oneembodiment, the composition of solubilized protein is prepared as aprotein powder using any suitable technique, including but not limitedto lyophilization, vacuum drying, freeze drying, spray drying, drumdrying, paddle-drying, super critical fluid processing, air drying, orother forms of evaporative drying. The drying step may be carried outany suitable temperature, for example, with respect to freeze drying, apreferred temperature range is from about 23° C. to about 40° C., with27° C. being the more preferred temperature.

The present invention is advantageous in that multiple components areefficiently and economically solubilized from the eggshell membrane atthe same time. Additionally, if desired, one or more specific componentsmay be isolated from the solubilized eggshell membrane, such as elastin,collagen or desmosine. Thus, the present invention allows for theproduction of a composition of a specific component or combination ofselected components in amounts suitable for use in a particularapplication. Thus, the composition may be customized for use in aparticular product, for example, a cosmetic product or a dietarysupplement. Advantageously, the compositions of the present inventionare essentially odor-free.

Once the proteinaceous material or source is solubilized, one skilled inthe art would be able to readily use standard biochemistry techniquessuch as membrane filtration or chromatography to isolate a protein ofinterest. Accordingly, the process of the invention may also includeisolating from the supernatant or dried solubilized composition variousproteins and polysaccharides of interest depending on the source of thestarting proteinaceous material. For example, proteins of interest thatmay be isolated from solubilized avian eggshell membrane include but arenot limited to elastin, desmosine, lysozyme, ovotransferrin,B-N-acetylglucosaminidase, collagen such as Type I collagen, Type Vcollagen, Type X collagen, or combinations thereof or other products ofinterest. Polysaccharides of interest that may be isolated include butare not limited to hyaluronic acid, glucosamine, and chondroitin.

In one embodiment, a soluble protein composition may be obtained frommethods of the present invention. In one aspect, the protein compositionmay include elastin, glucosamine, chondroitin, desmosine,ovotransferrin, B-N-acetylglucosaminidase, collagen such as Type Icollagen, Type V collagen, and/or Type X collagen, amino acids orcombinations thereof. The amino acids present in the composition mayinclude tryptophan, cystine, methionine, aspartic acid, threonine,serine, glutamic acid, proline, glutamic acid, proline, glycine,alanine, valine, isoleucine, tyrosine, phenylalanine, lysine, histidine,arginine, hydroxyproline and the like. The composition may also includehyaluronic acid, glucosamine, and chondroitin. In one aspect, thecomposition is more than 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or95% protein per weight of composition. In one aspect, the compositionincludes at least 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%,65%, 70%, 75% or 80% collagen and/or least 1% elastin. Of the collagenpresent, the collagen may be 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%,50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or 95% of Type I collagen.The composition may include 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90% or 95% of Type V collagen. The collagen of the composition maybe 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%,40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or 95% of Type Xcollagen. The amount of elastin in the composition may vary depending onthe size of membrane used to isolate the solubilized proteins. As shownin FIGS. 2 and 3, the composition may contain at least 10%, 15%, 20%,25%, 30%, 35% or even 40% elastin. In one embodiment, the inventionincludes an isolated, soluble protein composition that is at least 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90%, 95%, 96%, 97%, 98% or 99% soluble. The composition or proteinis “soluble” or “solubilized” if at least at least 10% (by weight) ofthe protein or composition dissolves or does not aggregate in distilledwater. Preferably, solubility of the protein or composition is assessedin distilled water, for example, at a concentration of 1 gram of theprotein or composition per 9 grams of distilled water.

The failure to develop a commercially feasible process of solubilizingvarious components from eggshell membrane is due in part to failure byothers to demonstrate high yields of a product in a highly purified,soluble form and that has retained bioactivity. As used interchangeablyherein, a “bioactivity”, “biological activity” or “native activity”,refers to a function exerted by an intact, non-dentatured protein,polypeptide or peptide as determined in vivo, or in vitro, according tostandard techniques. As described herein, the compositions of thepresent invention may be obtained from eggshell membranes without theuse of proteolytic enzymes or cross-linking agents. Accordingly, thesolubilized protein compositions are believed to be substantially pure,undenatured and retain biological activity.

Accordingly, a method of the present invention includes treating ananimal or human in need of a component solubilized from eggshellmembrane, e.g. protein, peptides, or amino acids, by administering acomposition of the present invention. The invention also provides amethod of treating a variety of diseases, disorders, and conditions thatbenefit from an effective amount of one or more components obtained fromsolubilized eggshell membrane. As used herein, unless otherwise definedin conjunction with specific diseases or disorders, the term “treating”refers to: (i) preventing a disease, disorder or condition fromoccurring in an animal or human that may be predisposed to the disease,disorder and/or condition but has not yet been diagnosed as having it;(ii) inhibiting the disease, disorder or condition, i.e., arresting itsdevelopment; and/or (iii) relieving the disease, disorder or condition,i.e., causing regression of the disease, disorder and/or condition.Accordingly, the composition or components, e.g. proteins, isolatedthereof may be used in any number of applications, including but notlimited to products or services in the cosmetic industry, see, forexample, U.S. Pat. No. 7,169,379 to Kouzuki; products in the healthindustry, for example, products for use in joint health; and products inthe medical industry, such as for wound healing, see U.S. Pat. No.7,041,868 to Greene. Such applications are known in the art as well asthe appropriate techniques for inclusion in such applications.

Accordingly, the present invention also relates to any pharmaceutical,dermatological, medical, nutritional or cosmetic compositions comprisinga component obtained from eggshell membrane using a process of thepresent invention. The composition may include an effective amount of atleast one or more components obtained from solubilized eggshellmembrane. As the diseases, disorders or conditions that would benefitfrom these compositions are well known, the compositions may be designedsuch that they contain appropriate levels effective for treatment of theparticular disease, disorder or condition. The compositions maygenerally be used in any formulation that is effective for treatment andthe intended mode of administration. For example, compositions ofelastin or collagen such as Type I collagen, Type V collagen, and/orType X collagen, for use in dermatological or cosmetic treatments may beformulated in topical or injectable forms and the like. Compositionscomprising solubilized proteins for use in nutritional or medicalapplications may be formulated in any suitable form, e.g. aqueous ordried, and administered by any effective route, such as orally orintramuscularly. As appreciated by one skilled in the art, compositionsof the present invention can be administered in a variety of waysincluding oral, enteral, parenteral, topical, sublingual, by inhalationspray, rectal and other appropriate routes of administration, such asoral, subcutaneous, transdermal, transmucosal, iontophoretic,intravenous, intramuscular, intraperitoneal, intranasal, subdural,rectal, and the like.

Compositions containing solubilized components from eggshell membranesof the present invention may be in any form suitable for the intendedmode of administration, including, for example, a powder, a solution, asuspension, or an emulsion. Liquid carriers are typically used inpreparing solutions, suspensions, and emulsions. Liquid carrierscontemplated for use in the practice of the present invention include,for example, water, saline, pharmaceutically acceptable organicsolvent(s), pharmaceutically acceptable oils or fats, and the like, aswell as mixtures of two or more thereof. The liquid carrier may containother suitable pharmaceutically acceptable additives such assolubilizers, emulsifiers, nutrients, buffers, preservatives, suspendingagents, thickening agents, viscosity regulators, stabilizers, and thelike. Suitable organic solvents include, for example, monohydricalcohols, such as ethanol, and polyhydric alcohols, such as glycols.Suitable oils include, for example, soybean oil, coconut oil, olive oil,safflower oil, cottonseed oil, and the like. For parenteraladministration, the carrier can also be an oily ester such as ethyloleate, isopropyl myristate, and the like. Compositions of the presentinvention may also be in the form of microparticles, microcapsules,liposomal encapsulates, and the like, as well as combinations of any twoor more thereof.

The compositions of the present invention may be administered orally,parenterally, sublingually, by inhalation spray, rectally, or topicallyin dosage unit formulations containing conventional nontoxicpharmaceutically acceptable carriers, adjuvants, and vehicles asdesired. Topical administration may also involve the use of emulsions,creams, ointments, transdermal patches or ionophoresis devices. The termparenteral as used herein includes subcutaneous injections, intravenous,intramuscular, intrasternal injection, or infusion techniques.

Injectable preparations, for example, sterile injectable aqueous oroleaginous suspensions may be formulated according to the known artusing suitable dispersing or wetting agents and suspending agents. Thesterile injectable preparation may also be a sterile injectable solutionor suspension in a nontoxic parenterally acceptable diluent or solvent,for example, as a solution in 1,3-propanediol. Among the acceptablevehicles and solvents that may be employed are water, Ringer's solution,and isotonic sodium chloride solution. In addition, sterile, fixed oilsare conventionally employed as a solvent or suspending medium. For thispurpose any bland fixed oil may be employed including synthetic mono- ordiglycerides. In addition, fatty acids such as oleic acid find use inthe preparation of injectables.

Suppositories for rectal administration of the drug can be prepared bymixing the drug with a suitable nonirritating excipient such as cocoabutter and polyethylene glycols that are solid at ordinary temperaturesbut liquid at the rectal temperature and will therefore melt in therectum and release the drug.

Solid dosage forms for oral administration may include capsules,tablets, pills, powders, and granules. In such solid dosage forms, theactive compound may be admixed with at least one inert diluent such assucrose lactose or starch. Such dosage forms may also comprise, as isnormal practice, additional substances other than inert diluents, e.g.,lubricating agents such as magnesium stearate. In the case of capsules,tablets, and pills, the dosage forms may also comprise buffering agents.Tablets and pills can additionally be prepared with enteric coatings.

Liquid dosage forms for oral administration may include pharmaceuticallyacceptable emulsions, solutions, suspensions, syrups, and elixirscontaining inert diluents commonly used in the art, such as water. Suchcompositions may also comprise adjuvants, such as wetting agents,emulsifying and suspending agents, cyclodextrins, and sweetening,flavoring, and perfuming agents.

This invention can be better understood by reference to the followingnon-limiting examples. It will be appreciated by those skilled in theart that other embodiments of the invention may be practiced withoutdeparting from the spirit and the scope of the invention as hereindisclosed and claimed.

EXAMPLE

The present invention is further defined in the following Examples, inwhich parts and percentages are by weight and degrees are Celsius,unless otherwise stated. The disclosure of each reference set forthherein is incorporated herein by reference in its entirety.

Example 1

Shown below is data resulting from the analysis of various samples ofthe resulting protein composition obtained by solubilizing avianeggshell membrane using a process of the present invention.

As indicated below, the solubilized protein composition was spray dried(SD), freeze dried (FD), or paddle dried (PD). Paddle dried is a commontechnique used by some egg breaking facilities to dry eggshells on acommercial scale.

The total protein (TP) concentration of the solubilized proteincomposition was measured using Leco instruments (St Joseph, Mich.)following the Association of Analytical Chemists (AOAC) protein bycombustion method 990.03. The solubilized protein composition wasdetermined “as is” in its current physical state as well as on a “drybasis”.

The ash content was determined using AOAC method 942.05. The percentsolubility of the resulting protein composition was determined usingstandard techniques. The percent collagen, elastin and sulfated glycanswere determined using various commercially available assays, forexample, colorimetric kits such as Sircol, Fastin, Blyscan assays(Biocolors Ltd, Northern Ireland). Percent hyaluronic acid wasdetermined by measuring uronic acid by a carbazole method. The aminoacid profile was performed by Eurofins Scientific, Inc. (Des Moines,Iowa). A Standard Plate Count (SPC) procedure was used to determine thepresence of bacteria in each of the samples, as indicated below by SPC.

The measurement of color was determined using the Hunter L, a, bstandard color scale, which is described below. Hunter L, a, b valuesare standard color scale values that indicate differences in brightness,hue and saturation using a standard color system which relates lightnessas L values, and hue and croma as a combination of a and b values on acoordinate scale, where a represents redness-greenness and b representsyellowness-blueness. L values describe the degree of darkness, where avalue of 100 equals white and that of 0 equals black, a-values describethe degree of redness, which increases with an increasing a-value.b-values describe the degree of yellowness, which increases withincreasing b-value. L, a, b and opacity theory and measurement arefurther described in the Hunter Lab Instruction Manual Hunter. L, a, band color scale values and opacity may be measured using a colorimeteravailable from Hunter Associate Laboratory, Inc. of Reston, Va., U.S.A.or the Color Machine Model 8900 available from Pacific Scientific.

As shown in FIG. 2, wet, dry or frozen membranes were put into astainless (316) tank and 12% NaOH was added and the mixture wasincubated at 32-40° C. overnight. After hydrolysis the mixture wascooled to 38-45° F. to slow continued hydrolysis. The mixture wascentrifuged to separate eggshells from solubilized proteins. Thecentrifuged solubilized proteins were then dialyzed through 3,000 MWCOmembranes until ash was reduced to a conductivity reading of 2-4 mS/cm.The proteins were then pH adjusted with 12% acetic acid to a pH of6.8-8. The pH adjusted protein mixture was then concentrated to a solidscontent of 25% to 30% at which time it could be spray dried or freezedried. Tables 1 and 2 below show the percent analysis of samples fromthe resulting composition.

TABLE 1 Percent analysis of sample compositions. Type (SD, Leco TP %Leco TP % Ash % Ash % Moist Solids Solubility Collagen Sample FD, PD)as-is dry basis as-is dry basis % % % % 1 FD 90.45 94.50 6.67 6.97 4.2995.71 95.40 16.96 2 FD 91.56 95.64 6.96 7.27 4.27 95.73 92.26 18.49 3 FD90.25 92.61 7.35 7.54 2.55 97.45 99.70 17.62 4 SD 91.66 100.03 6.22 6.798.37 91.63 98.16 15.44

TABLE 2 Percent analysis of sample compositions. Hyaluronic ElastinSulfated SPC's Salmonella Color Color Color Sample Acid % % Glycans %(cfu's/g) (neg/25 g) (L) (a) (b) 1 0.13 29.52 ND <100 neg 63.41 2.4118.88 2 0.17 24.20 ND <100 neg 63.78 3.35 20.64 3 0.15 22.50 0.01 1,800neg 57.47 0.57 15.42 4 0.20 24.52 ND <1,000 neg 86.37 −0.48 11.08

As shown in FIG. 3, various soluble protein compositions may be obtainedusing various membrane sizes in accordance with the methods of thepresent invention. A typical test analysis of the compositions obtainedfrom processing 600 pounds of eggshell membranes using various sizedmembranes are shown in Tables 3-6.

Example 2 Process for making the product referred to as Composition A inFIG. 3 a

The process for making the product referred to as Composition A includesadding eggshell membranes (wet, dry or frozen) to a jacketed 316stainless tank followed by 5% sodium hydroxide. The tank contents wereheated to 50° C. while stirring until hydrolysis was completed which is3 to 4 hours. The tank stirrer was shut off after hydrolysis wascomplete and eggshell is allowed to settle out. (Approx. 30 min.)Hydrolysis was monitored until no membrane was visible and only theeggshell remains.

The hydrolyzed membrane was pumped through a 250-500 μm membrane andinto the centrifuge for separation of eggshell fines from thesupernatant liquid.

After centrifuging, the supernatant liquid was pumped into a 1,000Dalton to 10,000 Dalton membrane system, where the ash was removed untilit measures less than 4 milliSiemens/cm at which time the pH wasadjusted to pH 6.8-7.6 with 0.5% acetic acid and dialyzed with one morevolume of water. The dialyzed, pH adjusted supernatant was concentratedto 20-30% solids and then spray dried in a nozzle dryer to generateComposition A. FIG. 3A and Table 3 below shows the resultingcomposition.

TABLE 3 Percent analysis of components of Composition A. Composition AAnalysis % Total protein 92.59 Ash 6.51 Moisture 5.00 Solids 95.01Collagen 32.17 Hyaluronic Acid 1.59 Elastin 21.62

Further analytical results indicate that the following amino acids arepresent in the following Composition A:

TABLE 4 Percent analysis of amino acid present in the Composition A.Amino Acid (%) Tryptophan 3.53 Cystine 2.47 Methionine 3.79 AsparticAcid 8.33 Threonine 3.08 Serine 3.30 Glutamic Acid 14.61 Proline 9.85Glycine 4.38 Alanine 2.25 Valine 7.51 Isoleucine 3.47 Leucine 4.72Tyrosine 1.72 Phenylalanine 1.57 Total Lysine 5.99 Histidine 3.23Arginine 6.58 Hydroxyproline 0.22

Example 3 Process for making the product referred to as Composition B inFIG. 3 a

Egg membranes (wet, dry or frozen) were added to a jacketed 316stainless tank followed by 5% sodium hydroxide. The tank contents wereheated to 50° C. while stirring until hydrolysis was completed which is3 to 4 hours. The tank stirrer was shut off after hydrolysis wascomplete and eggshell is allowed to settle out. (Approx. 30 min.)Hydrolysis was monitored until no membrane is visible and only theeggshell remains.

The hydrolyzed membrane is pumped through a 250-500 μm membrane and intothe centrifuge for separation of eggshell fines from the supernatantliquid.

After centrifuging, the hydrolyzed membrane was diafiltered through a100,000 molecular weight cutoff membrane. The retentate was saved andconductivity was reduced from 140 milliSiemens/cm to 4 milliSiemens/cmand concentrated to 25-30% solids and spray dried. The results are shownin the following table and in FIG. 3A.

TABLE 5 Percent analysis of components of the Composition B composition.Composition B Analysis % Total protein 94.10 Ash 6.67 Moisture 4.27Solids 95.73 Collagen 23.70 Hyaluronic Acid 1.27 Elastin 37.95

Example 4 Process for making the product referred to as Composition C inFIG. 3 b

The permeate was collected from the 100,000 molecular weight cutoffmembranes and dialyzed with 10,000 molecular weight membranes.Conductivity was reduced from 140 milliSiemens/cm to 4 milliSiemens/cmand concentrated to 25-30% solids and spray dried. The resultingcomposition is provided in FIG. 3B and Table 6 below.

TABLE 6 Percent analysis of components of the Composition C composition.Composition C Analysis % Total protein 90.18 Ash 8.09 Moisture 5.14Solids 94.86 Collagen 15.93 Hyaluronic Acid 2.00 Elastin 2.35

All publications and patent applications in this specification areindicative of the level of ordinary skill in the art to which thisinvention pertains. All publications and patent applications are hereinincorporated by reference to the same extent as if each individualpublication or patent application was specifically and individuallyindicated by reference.

The invention has been described with reference to various specific andpreferred embodiments and techniques. However, it should be understoodthat many variations and modifications may be made while remainingwithin the spirit and scope of the invention. In particular, it is to beunderstood that the present invention contemplates variations in theproteinaceous material, process parameters, including temperature, time,pH, salt (ash), separation techniques, drying or preparation techniques,and proteins of interest.

1. A method of treating an individual in need of proteins obtained fromeggshell membrane which comprises administering to said individual acomposition comprising proteins solubilized from eggshell membrane. 2.The method of claim 1, wherein the composition is prepared by a processcomprising subjecting the eggshell membrane to a sufficient amount of abasic solution to obtain a supernatant that has a basic pH; exposing thesupernatant to the basic solution for a sufficient length of time andtemperature for hydrolysis of the eggshell membrane to occur; andcooling the temperature of the supernatant comprising the mixture ofeggshell membranes and basic solution to obtain a composition ofsolubilized proteins.
 3. The method of claim 2, further comprisingacidifying the supernatant.
 4. The method of claim 1, wherein thecomposition is greater than 50% solubilized protein per weight of thecomposition and comprises Type I collagen, Type V collagen, Type Xcollagen, elastin, desmosine, lysozyme, ovotransferrin, orB-N-acetylglucosaminidase or combinations thereof.
 5. The method ofclaim 1 wherein the composition of proteins solubilized from eggshellmembrane is administered by a mode of administration selected from thegroup consisting of oral, subcutaneous, transdermal, transmucosal,iontophoretic, intravenous, intrathecal, buccal, sublingual, intranasal,and rectal administration.
 6. The method of claim 1 wherein theindividual is an animal or a human.
 7. The method of claim 1 furthercomprising treating an individual for joint health.